EMQN best practice guidelines for the molecular genetic testing and reporting of chromosome 11p15 imprinting disorders: Silver–Russell and Beckwith–Wiedemann syndrome

Katja Eggermann, Jet Bliek, Frédéric Brioude, Elizabeth Algar, Karin Buiting, Silvia Russo, Zeynep Tümer, David Monk, Gudrun Moore, Thalia Antoniadi, Fiona Macdonald, Irène Netchine, Paolo Lombardi, Lukas Soellner, Matthias Begemann, Dirk Prawitt, Eamonn R Maher, Marcel Mannens, Andrea Riccio, Rosanna Weksberg, Pablo Lapunzina, Karen Grønskov, Deborah JG Mackay, Thomas Eggermann

Open source

DOI: 10.1038/ejhg.2016.45
Published: 2016-05-11
Container: European Journal of Human Genetics
Publisher: Springer Science and Business Media LLC
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.1038/ejhg.2016.45,
  title = {EMQN best practice guidelines for the molecular genetic testing and reporting of chromosome 11p15 imprinting disorders: Silver–Russell and Beckwith–Wiedemann syndrome},
  author = {Katja Eggermann and Jet Bliek and Frédéric Brioude and Elizabeth Algar and Karin Buiting and Silvia Russo and Zeynep Tümer and David Monk and Gudrun Moore and Thalia Antoniadi and Fiona Macdonald and Irène Netchine and Paolo Lombardi and Lukas Soellner and Matthias Begemann and Dirk Prawitt and Eamonn R Maher and Marcel Mannens and Andrea Riccio and Rosanna Weksberg and Pablo Lapunzina and Karen Grønskov and Deborah JG Mackay and Thomas Eggermann},
  year = {2016},
  journal = {European Journal of Human Genetics},
  doi = {10.1038/ejhg.2016.45},
  url = {https://doi.org/10.1038/ejhg.2016.45}
}

RIS

TY  - JOUR
TI  - EMQN best practice guidelines for the molecular genetic testing and reporting of chromosome 11p15 imprinting disorders: Silver–Russell and Beckwith–Wiedemann syndrome
AU  - Katja Eggermann
AU  - Jet Bliek
AU  - Frédéric Brioude
AU  - Elizabeth Algar
AU  - Karin Buiting
AU  - Silvia Russo
AU  - Zeynep Tümer
AU  - David Monk
AU  - Gudrun Moore
AU  - Thalia Antoniadi
AU  - Fiona Macdonald
AU  - Irène Netchine
AU  - Paolo Lombardi
AU  - Lukas Soellner
AU  - Matthias Begemann
AU  - Dirk Prawitt
AU  - Eamonn R Maher
AU  - Marcel Mannens
AU  - Andrea Riccio
AU  - Rosanna Weksberg
AU  - Pablo Lapunzina
AU  - Karen Grønskov
AU  - Deborah JG Mackay
AU  - Thomas Eggermann
PY  - 2016
JO  - European Journal of Human Genetics
DO  - 10.1038/ejhg.2016.45
UR  - https://doi.org/10.1038/ejhg.2016.45
ER  -

APA

Eggermann, K., Bliek, J., Brioude, F., Algar, E., Buiting, K., Russo, S., Tümer, Z., Monk, D., Moore, G., Antoniadi, T., Macdonald, F., Netchine, I., Lombardi, P., Soellner, L., Begemann, M., Prawitt, D., Maher, E. R., Mannens, M., Riccio, A., Weksberg, R., Lapunzina, P., Grønskov, K., Mackay, D. J., & Eggermann, T. (2016). EMQN best practice guidelines for the molecular genetic testing and reporting of chromosome 11p15 imprinting disorders: Silver–Russell and Beckwith–Wiedemann syndrome. European Journal of Human Genetics. https://doi.org/10.1038/ejhg.2016.45

Source records

crossref · retrieved 2026-11-10T07:53:42.670Z